Slow Degradation Research Articles

Waste to health- seashells and pumpkin seeds into nanohydroxyapatite

Tonnes of pumpkin and piles of sea shells were amassed as waste products every year in the environment. Poor handling of waste can cause environmental pollution and globally initiatives have been made to take of them. Moreover, the focus on turning the waste into useful products hinders the dumping of waste and aids their management. Nanohydroxyapatite, a bioactive bone mineral, has emerged as an ideal candidate for bone substitution applications. The current study focuses on two main goals: waste management and the biogenic preparation of a value-added product, natural nanohydroxyapatite (Nat-Apatite). The seashells and Cucurbita maxima (Pumpkin seeds), which are often discarded as garbage, were utilized as a calcium source and phosphorous source, respectively. The Nat-Apatite exhibited a unique nanoglobular morphology and contained trace elements, such as strontium, magnesium, and sulphur. To assess the degradation rate of Nat-Apatite, we employed electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques. The results demonstrated a slow degradation rate, indicating potential compatibility with natural bone remodeling processes. Ex-vivo bone mineralization studies revealed that Nat-Apatite could promote nanoplatelet-like structures on decalcified bone surfaces. Furthermore, our study found that Nat-Apatite effectively enhanced the cell viability. Additionally, MG63 cells treated with Nat-Apatite showed increased production of calcium nodules, collagen, and alkaline phosphatase levels, suggesting improved osteogenic differentiation and bone formation. Thereby, the prepared Nat-Apatite can be potentially employed for biomedical applications.

New modifications of PBAT by a small amount of oxalic acid: Fast crystallization and enhanced degradation in all natural environments

Biodegradable plastics are often mistakenly thought to be capable of degrading in any environment, but their slow degradation rate in the natural environment is still unsatisfactory. We synthetized a novel series of poly(butylene oxalate-co-adipate-co-terephthalate) (PBOAT) with unchanged melting point (135 °C), high elastic modulus (140 - 219 MPa) and elongation at break (478 - 769%). Fast isothermal crystallization with a semi-crystallization time < 20 s was demonstrated by the PBOAT. In N2 and air atmospheres, the PBOAT maintained the Td,5% higher than 329 °C. They also had good thermal stability at melt processing temperature for more than 20 min. PBOAT exhibited faster hydrolysis and seawater degradation, even under natural soil burial without light, but still kept stable under low humidity conditions during the storage and the shelf-life. Moreover, the hydrolysis mechanisms were clarified based on Fukui function analysis and DFT calculation, indicating that the hydrolysis of PBOAT would be more straightforward. The mechanism of soil burial is also elucidated through detailed characterization of the structure changes. The PBOAT offered a fresh approach to the development of high-performing, naturally degradable materials.

Ratiometric fiber optic fluorescent pH sensor for hydroxide diffusion measurements in concrete

This article delineates the development of an advanced ratiometric pH optode designed for protracted monitoring of pH dynamics in cementitious materials—a crucial aspect of structural management. The optode features a dual-layer Hydromed™ D4 polymer pellet incorporating a pH-sensitive Naphth-AlkyneOMe fluorescent probe (pKa ≈ 12) and CdSe quantum dots as an internal reference. The polymer matrix, optimized with diamond powder and carbon black, enhances the signal while minimizing light artifacts. Demonstrating a robust response to pH fluctuations, the optode, utilizing ratiometric measurements, enables steadfast monitoring for up to 75 days.The experimental setup includes a Delrin® sample compartment housing a glass slide with the optode connected to an optical fiber via an SMA connector. HydroMed™ D4 films, forming the pH-sensitive layer, are deposited on the glass slide and secured. The optode configuration is fine-tuned to optimize signal intensity by reducing its length. For optode-detector coupling, a 1000 µm core diameter optical fiber links the optode, and a 405 nm LED illuminates the sensing film. The emission signal is collected through the optical fiber, and signals are processed using computer-controlled lock-in amplifiers.In the investigation of hydroxide ion diffusion through a concrete sample, the optode's efficacy was validated, aligning with pH electrode measurements. Addressing long-term stability, a degradation model uncovered leisurely kinetics with commendable stability. Slow degradation kinetics, with a reaction rate coefficient of 1.6 × 10⁻⁷ s⁻¹ and a half-life of 1180 h, exceeded expectations.This pH optode, showcasing an accurate and resilient response to pH variations within the 10 to 12.5 range, stands as a promising tool for monitoring pH dynamics in low-pH cementitious materials. The incorporation of a degradation model underscores fidelity over prolonged durations and offers a blueprint for enduring surveillance of concrete structures.

Using embossing ice particulate method to prepare polyvinyl alcohol/pullulan hydrogels with surface open pores loaded with microspheres for breast cancer treatment

In the post-operative treatment of breast cancer, early prevention of locoregional recurrence is crucial to avoid metastasis of cells from leftover microtumor tissues. The limitations in conventional drug delivery systems show a growing clinical demand for disease-specific drug-releasing systems. This study explores a novel poly(vinyl alcohol)/pullulan (PVA/PUL) hydrogel system for local drug delivery in post-operative breast cancer treatment. Hydrogel was produced by combination of lyophilization and embossing ice particulate techniques to create microspheres loaded open pores on the hydrogel surface for localized release of doxorubicin-loaded polycaprolactone microspheres (DOX-PCL-MSs). PVA/PUL hydrogel was successfully crosslinked with glutaraldehyde and stabilized hydrogel structure has possessed slow degradation rate and increasing water retention through 12 days. Release of DOX after 7 and 16 days from DOX-PCL-MSs loaded hydrogels were slower with a 6.2 ± 8.9 % and 56.6 ± 4.5 % release compared to 60.9 ± 14.6 % and 76.8 ± 19.7 % release from free DOX loaded hydrogel since DOX release was controlled by PCL microspheres. When interacted with human breast cancer cell line (MCF-7), DOX-PCL-MSs were able to disrupt cell and spheroid morphology after 7 days at concentrations as low as 12 μg/mL loaded DOX. In vitro cytotoxicity study has showed that, DOX-PCL-MSs loaded hydrogel was able to decrease MCF-7 viability after 7 days of incubation with controlled release of DOX. While free DOX releasing hydrogel has lost cytotoxic activity even after 4 days of incubation. Furthermore, ability of PVA/PUL hydrogel to support L929 cell attachment was shown in the study, suggesting hydrogels potential for promoting tissue regeneration after anti-cancer treatment. The study reveals that PVA/PUL hybrid hydrogels loaded with DOX-PCL-MSs has impactful potential in post-surgical treatment of breast cancer.

Magnesium Hydroxide as a Versatile Nanofiller for 3D-Printed PLA Bone Scaffolds.

Polylactic acid (PLA) has attracted much attention in bone tissue engineering due to its good biocompatibility and processability, but it still faces problems such as a slow degradation rate, acidic degradation product, weak biomineralization ability, and poor cell response, which limits its wider application in developing bone scaffolds. In this study, Mg(OH)2 nanoparticles were employed as a versatile nanofiller for developing PLA/Mg(OH)2 composite bone scaffolds using fused deposition modeling (FDM) 3D printing technology, and its mechanical, degradation, and biological properties were evaluated. The mechanical tests revealed that a 5 wt% addition of Mg(OH)2 improved the tensile and compressive strengths of the PLA scaffold by 20.50% and 63.97%, respectively. The soaking experiment in phosphate buffered solution (PBS) revealed that the alkaline degradation products of Mg(OH)2 neutralized the acidic degradation products of PLA, thus accelerating the degradation of PLA. The weight loss rate of the PLA/20Mg(OH)2 scaffold (15.40%) was significantly higher than that of PLA (0.15%) on day 28. Meanwhile, the composite scaffolds showed long-term Mg2+ release for more than 28 days. The simulated body fluid (SBF) immersion experiment indicated that Mg(OH)2 promoted the deposition of apatite and improved the biomineralization of PLA scaffolds. The cell culture of bone marrow mesenchymal stem cells (BMSCs) indicated that adding 5 wt% Mg(OH)2 effectively improved cell responses, including adhesion, proliferation, and osteogenic differentiation, due to the release of Mg2+. This study suggests that Mg(OH)2 can simultaneously address various issues related to polymer scaffolds, including degradation, mechanical properties, and cell interaction, having promising applications in tissue engineering.

Amphibian Segmentation Clock Models Suggest How Large Genome and Cell Sizes Slow Developmental Rate.

Evolutionary increases in genome size, cell volume, and nuclear volume have been observed across the tree of life, with positive correlations documented between all three traits. Developmental tempo slows as genomes, nuclei, and cells increase in size, yet the driving mechanisms are poorly understood. To bridge this gap, we use a mathematical model of the somitogenesis clock to link slowed developmental tempo with changes in intra-cellular gene expression kinetics induced by increasing genome size and nuclear volume. We adapt a well-known somitogenesis clock model to two model amphibian species that vary 10-fold in genome size: Xenopus laevis (3.1 Gb) and Ambystoma mexicanum (32 Gb). Based on simulations and backed by analytical derivations, we identify parameter changes originating from increased genome and nuclear size that slow gene expression kinetics. We simulate biological scenarios for which these parameter changes mathematically recapitulate slowed gene expression in A. mexicanum relative to X. laevis, and we consider scenarios for which additional alterations in gene product stability and chromatin packing are necessary. Results suggest that slowed degradation rates as well as changes induced by increasing nuclear volume and intron length, which remain relatively unexplored, are significant drivers of slowed developmental tempo.

Degradation and sorption of the herbicide pelargonic acid in subsoils below railway tracks compared to a range of topsoils

BackgroundPelargonic acid is a non-selective herbicide derived from natural sources with a range of potential applications in areas where synthetic herbicides may be less acceptable. One such use area is weed control on railway tracks. To assess the potential leaching of pelargonic acid to groundwater for this specific use, we conducted degradation and sorption studies with soils from railway tracks and, for comparison, with a range of topsoils.ResultsDegradation of pelargonic acid was very rapid in subsoils from railway tracks with half-lives (DT50) of < 1 day (geom. mean DT50, 5.8 h), and even faster in the selected agricultural topsoils (1.5 h). The starting concentration had a strong influence with much slower degradation at higher spike levels. Adsorption to the railway soils (alkaline soils with low organic matter content) was expectedly weak (Freundlich adsorption coefficients KF of 0.06–0.31 mL/g) and clearly stronger in the topsoils (0.2–40 mL/g). Organic carbon normalized adsorption coefficients (KFoc) ranged from 11 to 371 mL/g (all soils) and were pH dependent, consistent with the behaviour of weak acids. Computer modelling using the software PELMO and a set of scenarios for herbicide use on railway tracks developed for the authorisation in Germany yielded predicted environmental concentrations in groundwater of < 0.001 µg/L when parameterised with the adsorption and degradation endpoints from subsoils.ConclusionsThe leaching potential of pelargonic acid may be considered low even in application scenarios with sandy soils with low organic matter content such as those found below railway tracks.

Development of modified maize stover for enhancing soil nutrients and functional microbes: Application of NPK-enriched techniques

Returning maize stover (MS) to the soil can effectively enhance fertility by introducing organic matter. However, the slow degradation and nutrient deficiencies in MS potentially undermine soil quality. This study developed a method to synthesize NPK-enriched MS with the aim of improving soil nutrients and microbial diversity, as demonstrated in preliminary field trials. Under optimal conditions (8% urea, 4% KOH, and 8 freeze-thaw cycles), N and K were successfully grafted onto MS, forming MS-UK. This resulted in increased N and K content by 17.57% and 4.49%, respectively. The increase was due to urea interacting with fragmented lignin benzene rings to form C-N bonds, and KOH acting as a hydrogen bond acceptor to form C-K bonds. Following phosphorus adsorption with a K2HPO4 solution, MS-UK achieved a near-theoretical maximum adsorption capacity of 21.34 mg g−1, forming MS-UK-P. In field experiments, MS-UK-P showed a 29.11% higher degradation rate compared to unmodified MS. Notably, the MS-UK-P treatment group exhibited significant increases in soil organic carbon (SOC) and the availability of N, P, and K contents compared to the unmodified MS group, with SOC levels rising by 1.74 g kg−1, and N, P, and K contents increasing by 6.37 mg kg−1, 15.59 mg kg−1, and 18.7 mg kg−1, respectively. Furthermore, MS-UK-P promoted the growth of nitrogen and carbon-fixing microorganisms, including Bradyrhizobium, Gemmatimonadaceae, and Mycobacterium. This study highlights the urea-KOH and K2HPO4 modification as a novel and effective approach for converting MS into nutrient-rich fertilizer, offering new opportunities for enhancing the utilization of MS and similar agricultural residues to improve soil quality.

Fusarium biocontrol: antagonism and mycotoxin elimination by lactic acid bacteria.

Mycotoxins produced by Fusarium species are secondary metabolites with low molecular weight formed by filamentous fungi generally resistant to different environmental factors and, therefore, undergo slow degradation. Contamination by Fusarium mycotoxins in cereals and millets is the foremost quality challenge the food and feed industry faces across the globe. Several types of chemical preservatives are employed in the mitigation process of these mycotoxins, and they help in long-term storage; however, chemical preservatives can be used only to some extent, so the complete elimination of toxins from foods is still a herculean task. The growing demand for green-labeled food drives to evade the use of chemicals in the production processes is getting much demand. Thus, the biocontrol of food toxins is important in the developing food sector. Fusarium mycotoxins are world-spread contaminants naturally occurring in commodities, food, and feed. The major mycotoxins Fusarium species produce are deoxynivalenol, fumonisins, zearalenone, and T2/HT2 toxins. Lactic acid bacteria (LAB), generally regarded as safe (GRAS), is a well-explored bacterial community in food preparations and preservation for ages. Recent research suggests that LAB are the best choice for extenuating Fusarium mycotoxins. Apart from Fusarium mycotoxins, this review focuses on the latest studies on the mechanisms of how LAB effectively detoxify and remove these mycotoxins through their various bioactive molecules and background information of these molecules.

Nano-laponite encapsulated coaxial fiber scaffold promotes endochondral osteogenesis.

Osteoinductive supplements without side effects stand out from the growth factors and drugs widely used in bone tissue engineering. Lithium magnesium sodium silicate hydrate (laponite) nanoflake is a promising bioactive component for bone regeneration, attributed to its inherent biosafety and effective osteoinductivity. Up to now, the in vivo osteogenic potential and mechanisms of laponite-encapsulated fibrous membranes remain largely unexplored. This study presents a unique method for homogeneously integrating high concentrations of laponite RDS into a polycaprolactone (PCL) matrix by dispersing laponite RDS sol into the polymer solution. Subsequently, a core-shell fibrous membrane (10RP-PG), embedding laponite-loaded PCL in its core, was crafted using coaxial electrospinning. The PCL core's slow degradation and the shell's gradient degradation enabled the sustained release of bioactive ions (Si and Mg) from laponite. In vivo studies on a critical-sized calvarial bone defect model demonstrated that the 10RP-PG membrane markedly enhanced bone formation and remodeling by accelerating the process of endochondral ossification. Further transcriptome analysis suggested that osteogenesis in the 10RP-PG membrane is driven by Mg and Si from endocytosed laponite, activating pathways related to ossification and endochondral ossification, including Hippo, Wnt and Notch. The fabricated nanocomposite fibrous membranes hold great promise in the fields of critical-sized bone defect repair.

Intensity-Modulated Photocurrent Spectroscopy Measurements of High-Efficiency Perovskite Solar Cells.

Frequency domain characterization has long served as an important method for the examination of diverse kinetic processes that occur in solar cells. In this study, we investigated the dynamic response of high-efficiency perovskite solar cells utilizing ultra-low-intensity-modulated photocurrent spectroscopy. Distinctive intensity-modulated photocurrent spectroscopy (IMPS) attributes were detected only as a result of this low-intensity modulation, and their evolution under light and voltage bias was investigated in detail. We generally observed only two arcs in the Q-plane plots and attributed the smaller, low-frequency arc to trap-dominated charge transport in the device. Light and voltage bias-dependent measurements confirm this attribution. An equivalent circuit model was used to better understand the features and trends of these measurements and to validate our physical interpretation of the results. Additionally, we tracked the IMPS response of one of the cells over time and showed that slow degradation impacts the size and attributes of the low-frequency arc. Finally, we found that changes in the IMPS response correlate closely with the current versus voltage characteristics of the devices.

Strategies to Regulate the Degradation and Clearance of Mesoporous Silica Nanoparticles: A Review.

Mesoporous silica nanoparticles (MSNs) have attracted extensive attention as drug delivery systems because of their unique meso-structural features (high specific surface area, large pore volume, and tunable pore structure), easily modified surface, high drug-loading capacity, and sustained-release profiles. However, the enduring and non-specific enrichment of MSNs in healthy tissues may lead to toxicity due to their slow degradability and hinder their clinical application. The emergence of degradable MSNs provided a solution to this problem. The understanding of strategies to regulate degradation and clearance of these MSNs for promoting clinical trials and expanding their biological applications is essential. Here, a diverse variety of degradable MSNs regarding considerations of physiochemical properties and doping strategies of degradation, the biodistribution of MSNs in vivo, internal clearance mechanism, and adjusting physical parameters of clearance are highlighted. Finally, an overview of these degradable and clearable MSNs strategies for biosafety is provided along with an outlook of the encountered challenges.

Fine and Rough Structures of the Frequency Spectrum of a High-Power Laser Diodes during Slow Degradation

Fine and Rough Structures of the Frequency Spectrum of a High-Power Laser Diodes during Slow Degradation

A bilayer hydrogel mimicking the periosteum-bone structure for innervated bone regeneration.

In bone tissue, nerves are primarily located in the periosteum and play an indispensable role in bone defect repair. However, most bone tissue engineering approaches ignored the reconstruction of the nerve network. Herein, we aimed to develop a bilayer hydrogel simulating periosteum-bone structure to induce innervated bone regeneration. The bottom "bone" layer consisted of gelatin methacryloyl (GelMA), poly(ethylene glycol) diacrylate (PEGDA), and nano-hydroxyapatite (nHA), whereas the upper "periosteum" layer consisted of GelMA, sodium alginate (SA) and MgCl2. The mechanical properties of the upper and bottom hydrogels were designed to be suitable for neurogenesis and osteogenesis, respectively. Besides, Mg2+ from the "periosteum" layer released at the early stage (within 7 d), which aligned with the optimal time window for nerve regeneration and osteogenic related neuropeptide release. Simultaneously, the prevention of long-term Mg2+ release (after 7 d) could avoid osteogenic inhibition caused by prolonged Mg2+ exposure. Additionally, the incorporation of nHA in the bottom "bone" layer supported the long-term osteogenesis due to its osteoconductivity and slow degradation. In vitro biological experiments revealed that the bilayer hydrogel (GS@Mg/GP@nHA) promoted neurite growth and calcitonin gene-related peptide (CGRP) expression in rat dorsal root ganglion (DRG) neurons, as well as the osteogenesis of rat bone-derived mesenchymal stem cells (BMSCs). Moreover, the in vivo experiments demonstrated that the GS@Mg/GP@nHA hydrogel efficiently promoted nerve network reconstruction and bone regeneration of rat calvarial bone defects. Altogether, the bilayer hydrogel GS@Mg/GP@nHA could promote innervated bone regeneration, providing new insights for biomaterial design for bone tissue engineering.

Engineering hemin-loaded hyaluronan needle-like microparticles with photoprotective properties against UV-induced tissue damage.

This study aimed to develop hyaluronan (HA)-based hydrogel microparticles (MPs) loaded with hemin to address the limitations of traditional macroscale hydrogels. The objective is to design MPs such that they can modulate their physicochemical properties. Given the widespread use of ultraviolet C (UVC) light in various industries and the need for protective measures against accidental exposure, this study evaluated the potential of hemin-loaded MPs to protect human dermal fibroblasts from oxidative stress and cell death caused by UVC exposure. Multiple MP formulations were developed and analysed for size, surface charge, swelling behaviour, degradation rate, and radical scavenging capabilities, both with and without hemin loading. The most promising formulations were tested against UVC-exposed cells to assess cell viability, intracellular nitric oxide (˙NO) and reactive oxygen species levels, and protein carbonylation. The fabricated particles were in the form of microneedles, and the degree of their crosslinking and the role of hemin in the chemical crosslinking reaction were found to influence the surface charge and hydrodynamic diameter of the MPs. Increased crosslinking resulted in reduced swelling, slower degradation, and decreased hemin release rate. MPs with a higher degree of swelling were capable of releasing hemin into the culture medium, leading to enhanced bilirubin generation in dermal fibroblasts following cellular uptake. Pre-treatment with these MPs protected the cells from UVC-induced cell death, nitrosative stress, and protein carbonylation. These findings highlight the potential of the studied MPs to release hemin and to minimise the harmful effects of UVC on dermal fibroblasts.

Microbial degradation of bioplastic (PHBV) is limited by nutrient availability at high microplastic loadings

Biodegradable plastic offers an alternative to conventional plastic use in agriculture. However, slower degradation in the environment compared to industrial composting and high production of microplastics is of growing concern...

Bridging polymer architecture, printability, and properties by digital light processing of block copolycarbonates.

CO2-based aliphatic polycarbonates (aPCs), produced through the alternating copolymerization of epoxides with CO2, present an appealing option for sustainable polymeric materials owing to their renewable feedstock and degradable characteristics. An ongoing challenge in working with aPCs is modifying their mechanical properties to meet specific demands. Herein, we report that monomer ratio and polymer architecture of aPCs impact not only printability by digital light processing (DLP) additive manufacturing, but also dictate the thermomechanical and degradation properties of the printed objects. We found that block copolymers exhibit tailorable thermomechanical properties ranging from soft elastomeric to strong and brittle as the proportion of hard blocks increases, whereas the homopolymer blend failed to print objects and statistical copolymers delaminated or overcured, displaying the weakest mechanical properties. In addition, the hydrolytic degradation of the prints was demonstrated under various conditions, revealing that BCP prints containing a higher proportion of hard blocks had slower degradation and that statistical copolymer prints degraded more slowly than their BCP counterparts. This study underscores that polymer composition and architecture both play key roles in resin printability and bulk properties, offering significant prospects for advancing sustainable materials in additive manufacturing through polymer design.

Advance of Metal Compound Cathodes in Lithium Sulfur Batteries

With the rapid development of technology, people’s demand for energy is increasing day by day. Many energy devices electric vehicles and other technological products require high-energy lithium secondary batteries to operate. Higher electrochemical energy per unit volume and lower manufacturing cost than lithium batteries are the characteristic advantages of lithium sulfur (LiS) batteries. At the same time, it is environmentally friendly. The global reserves of elemental sulfur are also very abundant, and the cost is low. Therefore, LiS batteries have become one of the most promising secondary batteries in the future. However, LiS batteries also suffer from issues such as poor conductivity of the active substance sulfur, shuttle effect, volume expansion, and lithium dendrites. Research has found that the application of composite materials of metal compounds and sulfur in the cathode of LiS batteries can effectively limit the shuttle effect and poor conductivity of LiS batteries. It can effectively adsorb polysulfides generated in the reaction, optimize the electric performance of cathode sulfur, strengthen the rate performance and cycle stability of lithium ion battery, as well as reduce capacity degradation, significantly improving their electrochemical performance. This article reviews the research progress on the application of metal compounds, mainly metal oxides and metal sulfides, in the cathode of LiS batteries. It explores how this application can suppress shuttle effects and slow down capacity degradation and summarizes and looks forward to its development.

Degradation behavior of stressed polyester reinforcing products under alkaline conditions embedded in eluates and soils

The use of geosynthetic reinforcements in different applications has been proven over the last decades to be a very beneficial and valid technique. For a safe design of such structures the long-term behavior and especially the available resistant tensile force over the time under variable boundary conditions, such as temperature, chemical influences or loading conditions, has to be well known and understood. The known effects, which lead to a reduction in tensile strength, are considered in the design by applying so called reduction factors. So far, those reduction factors are determined separately without considering a possible interdependency. Latest research results are indicating that this can lead to major misjudgements. The main mechanism of the chemical degradation of polyester in high alkaline environment is the so called alkaline or “external” hydrolyses. In contrast to the internal hydrolyses, which provokes an evenly distributed, very slow degradation of the whole cross-section of the synthetic material, the external degradation generates a much faster “surface corrosion” with creation of fissures or cracks. If this does occur while the material is loaded, the fissures are widened, and their propagation are dramatically accelerated. The understanding and consideration of chemical degradation under mechanical stress is from crucial importance. This research will present results for products made of PET with different production technologies, where above-described mechanism has been investigated in more detail and conclude with a recommendation, how to proceed based on those findings. Tests have been conducted with samples embedded in eluate as well as in partially and fully saturated soils.

Creating equilibrium glassy states via random particle bonding

Creating amorphous solid states by randomly bonding an ensemble of dense liquid monomers is a common procedure that is used to create a variety of materials, such as epoxy resins, colloidal gels, and vitrimers. However, the properties of the resulting solid do a priori strongly depend on the preparation history. This can lead to substantial aging of the material; for example, properties such as mechanical moduli and transport coefficients rely on the time elapsed since solidification, which can lead to a slow degradation of the material in technological applications. It is therefore important to understand under which conditions random monomer bonding can lead to stable solid states, that is, long-lived metastable states whose properties do not change over time. This work presents a theoretical and computational analysis of this problem and introduces a random bonding procedure that ensures the proper equilibration of the resulting amorphous states. Our procedure also provides a new route to investigate the fundamental properties of glassy energy landscapes by producing translationally invariant ultrastable glassy states in simple particle models.